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WO1998039054A1 - Catheter a canal de fil de guidage etirable - Google Patents

Catheter a canal de fil de guidage etirable Download PDF

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Publication number
WO1998039054A1
WO1998039054A1 PCT/US1998/004282 US9804282W WO9839054A1 WO 1998039054 A1 WO1998039054 A1 WO 1998039054A1 US 9804282 W US9804282 W US 9804282W WO 9839054 A1 WO9839054 A1 WO 9839054A1
Authority
WO
WIPO (PCT)
Prior art keywords
elongated
lumen
balloon
catheter
guide member
Prior art date
Application number
PCT/US1998/004282
Other languages
English (en)
Inventor
Steven P. Mertens
Brent C. Gerberding
David J. Blaeser
Original Assignee
Scimed Life Systems, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Scimed Life Systems, Inc. filed Critical Scimed Life Systems, Inc.
Publication of WO1998039054A1 publication Critical patent/WO1998039054A1/fr

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M25/104Balloon catheters used for angioplasty
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M2025/0004Catheters; Hollow probes having two or more concentrically arranged tubes for forming a concentric catheter system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0043Catheters; Hollow probes characterised by structural features
    • A61M25/0045Catheters; Hollow probes characterised by structural features multi-layered, e.g. coated
    • A61M2025/0046Coatings for improving slidability
    • A61M2025/0047Coatings for improving slidability the inner layer having a higher lubricity
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/0074Dynamic characteristics of the catheter tip, e.g. openable, closable, expandable or deformable
    • A61M2025/0079Separate user-activated means, e.g. guidewires, guide tubes, balloon catheters or sheaths, for sealing off an orifice, e.g. a lumen or side holes, of a catheter
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M2025/0098Catheters; Hollow probes having a strain relief at the proximal end, e.g. sleeve
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/01Introducing, guiding, advancing, emplacing or holding catheters
    • A61M2025/0175Introducing, guiding, advancing, emplacing or holding catheters having telescopic features, interengaging nestable members movable in relations to one another
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/01Introducing, guiding, advancing, emplacing or holding catheters
    • A61M2025/0183Rapid exchange or monorail catheters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M2025/1043Balloon catheters with special features or adapted for special applications
    • A61M2025/1056Balloon catheters with special features or adapted for special applications having guide wire lumens outside the main shaft, i.e. the guide wire lumen is within or on the surface of the balloon
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M2025/1043Balloon catheters with special features or adapted for special applications
    • A61M2025/1063Balloon catheters with special features or adapted for special applications having only one lumen used for guide wire and inflation, e.g. to minimise the diameter
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M2025/1043Balloon catheters with special features or adapted for special applications
    • A61M2025/1079Balloon catheters with special features or adapted for special applications having radio-opaque markers in the region of the balloon
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M2025/1043Balloon catheters with special features or adapted for special applications
    • A61M2025/1093Balloon catheters with special features or adapted for special applications having particular tip characteristics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/0068Static characteristics of the catheter tip, e.g. shape, atraumatic tip, curved tip or tip structure
    • A61M25/0069Tip not integral with tube
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/008Strength or flexibility characteristics of the catheter tip
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0067Catheters; Hollow probes characterised by the distal end, e.g. tips
    • A61M25/0082Catheter tip comprising a tool

Definitions

  • the present invention relates generally to methods and devices used in intravascular therapeutic and diagnostic procedures. More particularly, the present invention relates to methods and apparatus for providing therapeutic and/or diagnostic devices to a desired vascular site through a dilation balloon catheter, while allowing the dilatation balloon catheter to be withdrawn from the desired area.
  • Intravascular therapeutic techniques such as angioplasty procedures, have been developed as alternatives to bypass surgery for treating vascular diseases or other conditions that occlude or reduce the lumen size of portions of a patient's vascular system.
  • a balloon catheter is typically inserted intravascularly into a patient through a relatively small puncture, which may be located proximate the groin, and navigated by a treating physician to the occluded vascular site.
  • a balloon catheter typically includes a balloon or dilating member at the distal end which is placed adjacent the vascular occlusion. Intravascular inflation of the dilating member by sufficient pressures, on the order of 5 to 12 atmospheres or so, causes the balloon to displace the occluding matter. It is known that a number of sequential balloon dilatations may be required to properly revascularize the occluded lumen and restore substantially normal blood flow therethrough. Because the effectiveness of any one balloon dilatation may not be known, it is desirable to view the vascular site after selected balloon dilations to monitor the progress and to determine if any adjustments should be made to the procedure.
  • One known method for viewing the vascular site is to inject a radiopaque die into the patient's vasculature. X-rays or the like may then be used to view the revascularized portion of the vessel.
  • a disadvantage of this approach is that extended exposure to X- rays can be harmful to both the patient and the treating personnel.
  • IVUS Intra-Vascular Ultra-Sonic
  • the IVUS device can be advanced down the guide wire lumen of a balloon dilatation catheter until the IVUS device is adjacent the dilatation balloon. After a selected balloon dilatation, the IVUS device may provide an image of the revascularized portion of the vessel.
  • a limitation of this approach is that the dilatation balloon often distorts the ultra-sonic image of the vessel, and thus the usefulness of the images provided by the IVUS device are negated.
  • the present invention overcomes many of the limitations of the prior art by providing a method and apparatus for introducing therapeutic and/or diagnostic devices through a balloon dilatation catheter and to an occluded vessel, while allowing the balloon dilatation catheter to be withdrawn from the desired area.
  • This may enable, for example an Intra-Vascular Ultra-Sonic (IVUS) device, to produce non-distorted images of a revascularized portion of a vessel.
  • IVUS Intra-Vascular Ultra-Sonic
  • a longitudinally extendable guide member is provided in a balloon dilatation catheter. Positioned within the longitudinally extendable guide member is preferably a therapeutic and/or diagnostic device, such as an IVUS device.
  • a therapeutic and/or diagnostic device such as an IVUS device.
  • the balloon is positioned adjacent an occluded site and inflated to dilate the occluding matter. Thereafter, and to view the revascularized portion of the vessel, the IVUS device may be advanced down the extendable guide member until the IVUS device is adjacent the desired site.
  • the balloon dilatation catheter may be pulled proximally relative to the extendable guide member.
  • the dilatation balloon is effectively moved proximally away from the IVUS device, while the IVUS device remains adjacent the revascularized portion of the vessel. That is, and in a preferred embodiment, the extendable guide wire lumen member and the IVUS device remain substantially stationary relative to the revascularized portion of the vessel.
  • the IVUS device may then be used to provide an image of the revascularized portion of the vessel. It is noted that the extendable guide member may provide protection to the IVUS device while the balloon dilatation catheter is withdrawn proximally therefrom.
  • the balloon catheter may easily be repositioned across the site by simply re-advancing the balloon catheter over the extendable guide member. This configuration provides an efficient means for dilating a vessel with a dilation balloon, and imaging the vessel between selected dilatations.
  • the balloon dilatation catheter includes an inflation tube with an inflation lumen extending therethrough. Attached to a distal end portion of the inflation tube is an inflatable balloon. The interior of the inflatable balloon is in fluid communication with the inflation lumen of the inflation tube. In this configuration, the inflatable balloon can be expanded by applying pressure to the inflation lumen.
  • an elongated guide member preferably coextends interiorly within at least a portion of the inflation lumen of the balloon catheter, and is in a slidable relation therewith. The elongated guide member is also adapted to slidably receive an elongated device such as an IVUS device.
  • a sealing means is provided in the balloon catheter.
  • the sealing means slidably receives the guide member and provides a seal between the inflation lumen and the exterior of the intravascular catheter. The seal thus allows the guide member to be longitudinally slidable relative to the balloon catheter while enabling the dilatation balloon to be inflated when desired.
  • the sealing means comprises a seal between the inflation tube and the guide member.
  • the guide member may be slidably positioned relative to the dilatation balloon.
  • an IVUS device that is positioned within the guide member may be slidably positioned relative to the dilatation balloon, and in particular, selectively positioned distally of the dilatation balloon.
  • a first illustrative method includes the steps of: providing a catheter that has a movable guide member therein and a balloon located on the distal end thereof, wherein the catheter is positioned within the body such that the balloon is located adjacent the selected portion of the vessel; providing an elongated device that has an imaging device located near the distal end thereof, wherein the elongated device is positioned within the guide member; moving the catheter proximally of the selected portion of the vessel while leaving the movable guide member substantially stationary relative to the selected portion of the vessel; positioning the elongated device adjacent the selected portion of the vessel; and imaging the selected portion of the vessel with the imaging device.
  • a standard balloon catheter is combined with a lumen extension device.
  • the lumen extension device is a separate device that is used in conjunction with a catheter that has a guide wire lumen therein.
  • the lumen extension device allows a user to selectively extend the guide wire lumen of a conventional catheter.
  • the lumen extension device includes an elongated guide member for slidably receiving an elongated device, such as an IVUS device.
  • the guide member is adapted to be slidably disposed within the guide wire lumen of the standard catheter.
  • Attached to the proximal end of the guide member is a housing.
  • the housing preferably engages the proximal end of the catheter, and has a control mechanism for controlling the relative longitudinal position of the guide member relative to the catheter.
  • the catheter has a manifold on the proximal end thereof, and the housing is attached to the manifold.
  • another illustrative method including the steps of: providing a catheter that has a guide wire lumen extending longitudinally therethrough, and a balloon located on the distal end thereof, wherein the catheter is inserted into the body such that the balloon is positioned adjacent to the selected portion of the vessel; providing a lumen extension device comprising an elongated tube, wherein the lumen extension device is slidably positioned within the guide wire lumen of the catheter; providing an elongated device that has an imaging device located near the distal end thereof, wherein the elongated device is positioned within the elongated tube of the lumen extension device; moving the catheter proximally of the selected portion of the vessel while leaving the guide member of the lumen extension device substantially stationary relative to the selected portion of the vessel; positioning the elongated device adjacent the selected portion of the vessel; and imaging the selected portion of the vessel with the imaging device.
  • Figure 1 is a side view, partially in section, of a preferred embodiment of a balloon dilation catheter of the present invention
  • Figure 2 is a longitudinal sectional view of a distal portion of the catheter shown in Figure 1 ;
  • Figure 3 is a cross-sectional view of the catheter taken along the line 3-3 in Figure 1;
  • Figure 4 is a cross-sectional view of the catheter taken along the line 4-4 in Figure 2;
  • Figure 5 is a cross-sectional view of the catheter taken along the line 5-5 in Figure 2;
  • Figure 6 is a cross-sectional view of the catheter taken along the line 6-6 of Figure 2;
  • Figure 7 is a cross-sectional view of the catheter taken along the line 7-7 of
  • Figure 8 is a cross-sectional view of the catheter taken along the line 8-8 of Figure 2;
  • Figure 9 is a longitudinal sectional view of a second preferred embodiment of a balloon dilation catheter
  • Figure 9A is a longitudinal sectional view of an alternative embodiment of the catheter shown in Figure 9;
  • Figure 10 is a cross-sectional view of the second preferred embodiment taken along the line 10-10 in Figure 9;
  • Figure 11 is a cross-sectional view of the second preferred embodiment taken along the line 11-11 in Figure 9;
  • Figure 12 is a side view, partially in section, of a third preferred embodiment of a balloon dilation catheter showing a deflated balloon;
  • Figure 13 is a side view, partially in section, of the embodiment in Figure 12 showing an inflated balloon
  • Figure 14 is a side view, partially in section, of a fourth preferred embodiment of a balloon dilation catheter showing a deflated balloon;
  • Figure 15 is a side view, partially in section, of the embodiment in Figure 14 showing an inflated balloon
  • Figure 16 is a side view, partially in section, of a fifth preferred embodiment of a balloon dilatation catheter
  • Figure 17 is a cross-sectional view of the catheter taken along the line 17-17 in Figure 16;
  • Figure 18 is a cross-sectional view of the catheter taken along the line 18-18 in Figure 16;
  • Figure 19 is a cross-sectional view of the catheter taken along the line 19-19 in Figure 16;
  • Figure 20 is a side view, partially in section, of a sixth preferred embodiment of a balloon dilatation catheter;
  • Figure 21 is a side view, partially in section, of the embodiment shown in Figure
  • Figure 22 is a side view, partially in section, of a lumen extension device coupled with a conventional over-the-wire balloon dilatation catheter;
  • Figure 23 is a side view, partially in section, of the lumen extension device shown in Figure 22.
  • Detailed Description of the Preferred Embodiment The presently preferred embodiments and methodology described herein are applicable to coronary angioplasty procedures and are specifically described in the context of dilation balloon catheters. It should be understood, however, that the embodiments and methodology of the present invention may be adapted for use with other types of intravascular therapeutic devices, such as atherectomy catheters, as well as diagnostic catheters, such as ultrasonic catheters.
  • the intravascular apparatus 10 includes a balloon dilation catheter 12 having an elongated shaft 14.
  • a proximal portion 16 of the shaft 14 is adapted to extend outside the body of a patient during use, and a distal portion 18 of the shaft 14 is positionable intravascularly during use by manipulation of the proximal portion 16.
  • a dilation balloon 20 is located at and connected to the distal portion 18 of the catheter shaft 14.
  • the balloon 20 can be formed from a polyolefin copolymer or other polymer material.
  • the balloon 20 is formed of a polyolefin copolymer (such as that sold by DuPont under the tradename SURLYN as Resin No. 8527) using secondary treatment with 5 to 50 Mega-rad electron beam irradiation to enhance strength in the region of the balloon 20.
  • the balloon 20 has a proximal neck portion 22 defining a proximal opening 24, and a distal neck portion 26 defining a distal opening 28.
  • the proximal neck portion 22 preferably has an outer diameter of about 0.040 inches and an inner diameter of about 0.034 inches.
  • the distal neck portion 26 preferably has an outer diameter of about 0.030 inches and an inner diameter of about 0.025 inches.
  • the distal portion 18 of the shaft 14 extends into the proximal opening 24 in the balloon 20 and is preferably connected to the proximal neck portion 22.
  • the shaft 14 includes an inflation lumen 30 extending therethrough and has a proximal opening 32 and a distal opening 34.
  • a manifold 36 is connected to the proximal portion 16 of the shaft 14 and the dilation balloon 20 is in fluid flow communication with the inflation lumen 30. Inflation fluid is conveyed via the lumen 30 from the manifold 36 to inflate the balloon 20 and therefore dilate a vessel in a conventional manner known in the art.
  • the shaft 14 has a length of approximately 135 cm.
  • the proximal portion 16 of the shaft 14 is preferably made of stainless steel hypodermic tubing and the distal portion 18 is made of a relatively flexible polymeric material such as a polyolefin copolymer or polyethylene.
  • This type of shaft is disclosed in U.S. Patent Application Serial No. 07/833,099, filed February 10, 1992, the disclosure of which is specifically incorporated herein by reference.
  • the shape of the shaft 14 and lumen 30 converges from a circular cross-section at the proximal portion 16 thereof ( Figure 3) to a kidney-shaped cross section at the distal portion thereof ( Figures 4-6).
  • An upper wall 38 and a lower wall 40 of the shaft 14 converge distally of the distal opening 34 in the lumen 30 and extend across the balloon 20 to a position adjacent the distal neck portion 26 of the balloon 20.
  • a stiffening wire 42 extends distally from a distal end of the steel tubing and is attached to a distal end of the balloon 20 as disclosed in the '113 patent to provide additional support for the manipulation of the catheter 12.
  • the stiffening wire 42 can be attached to an underside of the upper wall 38 of the shaft and extend to approximately the center of the balloon 20 as shown in Figures 1 and 2.
  • an elongated guide lumen 44 is adapted to extend through the proximal and distal openings 24 and 28 of the balloon 20 for slidable movement relative to the balloon
  • the guide lumen 44 also has an inner chamber 50 extending therethrough from a proximal end 52 to a distal end 53 thereof for slidably receiving a conventional guide wire 54.
  • the guide lumen 44 has a sufficient length, preferably about 135 cm, so that a proximal portion 46 of the guide lumen 44 can extend outside the body of a patient during use while a distal portion 48 extends distally of the balloon 20.
  • the guide lumen 44 is approximately the same length as a conventional catheter.
  • the guide lumen 44 may also be provided in different sizes to accommodate different size devices.
  • the guide lumen 44 can be provided with an inner diameter of 0.017 inches and an outer diameter of 0.020 inches for use with a 0.014 inch guide wire.
  • the guide lumen 44 may be provided with an inner diameter of 0.013 inches and an outer diameter of 0.016 inches.
  • the guide lumen 44 is made of a polymeric material, such as polyimide, and has a low friction coating, such as Teflon®, on both the inner and outer surfaces thereof.
  • a coating on the inner surface enhances guide wire movement through the chamber 50, and a coating on the outer surface enhances movement of the guide lumen 44 through a guiding catheter, a vessel, or the balloon 20.
  • the guide lumen 44 can be made of other materials, such as polyurethane, polyester, or other polymers.
  • the guide lumen 44 can also be made of a polyimide-teflon composite material, or reinforced with wire or a braid of metal or plastic or other materials.
  • the pitch of a wound reinforcing wire can be varied a desired amount along the length of the guide lumen 44.
  • the variable pitch wire can provide increased stiffness at the proximal portion 46 of the guide lumen 44 to facilitate manipulation of the entire guide lumen 44.
  • the variable pitch wire can also provide sufficient flexibility at the distal portion 48 of the guide lumen 44 to allow the guide lumen 44 to easily follow the guide wire 54 through a vessel.
  • the coatings may be made of other materials such as a hydrophilic or silicone coating.
  • a metallic or foil coating may also be incorporated on the inner or outer surface of the guide lumen 44.
  • the guide wire 54 has a sufficient length, preferably about 160-190 cm, so that a proximal portion 56 of the guide wire 54 can extend outside the body of a patient from an opening in the proximal end 52 in the guide lumen 44 while a distal portion 58 extends distally from an opening in the distal end 53 of the guide lumen 44.
  • the proximal portion 56 of the guide wire 54 can also extend out of an opening in the guide lumen located distally of the proximal end 52 of the guide lumen 44.
  • a proximal seal member 62 is sealingly connected to the proximal neck portion 22 of the balloon 20 and a distal seal member 64 is sealingly connected to the distal neck portion 26 of the balloon 20.
  • the proximal and distal seal members 62 and 64 have passageways 66 and 68 therethrough for slidably receiving the guide lumen 44.
  • the seal members 62 and 64 are preferably configured as collars and are made of a polymeric material, such as polyimide, polyurethane, polyester or the like.
  • An upper portion of the proximal seal member 62 is attached to the curved bottom wall 40 of the catheter shaft 14, and a lower portion is attached to the proximal neck portion 22 of the balloon 20.
  • the entire periphery of the distal seal member 64 is attached to the distal neck portion 26, and a distal end 70 of the shaft 14 is attached to a top portion of the distal seal member 64 proximally of the neck portion 26.
  • the distal portion 48 of the guide lumen 44 is adapted to extend distally from an end 71 of the distal seal member 64 while the proximal portion 46 is outside the body of a patient.
  • the outer diameter of the guide lumen 44 is only slightly smaller than the inner diameters of the proximal and distal seal members 62 and 64 to create a tolerance fit which allows slidable movement of the guide lumen 44 through the seal member passageways 66 and 68.
  • the tolerance fit between the guide lumen 44 and the proximal and distal seal members 62 and 64 inhibits inflation fluid from exiting the balloon 20.
  • distal seal member 64 preferably extends proximally into the balloon 20 and has an expandable, tubular valve member 72 made of an elastomeric material such as TECOTHANE or the like. As shown in dashed lines in Figure 2, the valve member 72 expands radially inward against the guide lumen 44 when the balloon
  • valve 20 is inflated to further seal any space between the guide lumen 44 and the distal seal member 64.
  • a valve member of similar construction can also be incorporated into the proximal seal member 62 if desired.
  • a longitudinally extendable guide lumen 44 is provided in the distal seal member 64.
  • a therapeutic and/or diagnostic device 54 such as an IVUS device.
  • the balloon 20 is positioned adjacent an occluded site and inflated to dilate the occluding matter. Thereafter, the intravascular apparatus 10 may be withdrawn relative to the vessel while the guide lumen 44 and the IVUS device 54 may remain substantially at the revascularized portion of the vessel.
  • the dilatation balloon 20 may be effectively moved proximally away from the IVUS device 54 and the guide lumen 44, while the IVUS device 54 and the guide lumen 44 remain substantially adjacent the revascularized portion of the vessel.
  • the IVUS device 54 may then be used to provide an image of the revascularized portion of the vessel.
  • the extendable guide lumen 44 may provide protection to the IVUS device 54 while the intravascular apparatus 10 is withdrawn proximally therefrom.
  • the intravascular apparatus 10 may easily be repositioned across the site by simply advancing the intravascular apparatus 10 over the extendable guide lumen 44.
  • This configuration provides an efficient means for dilating a vessel with a dilation balloon, and imaging the vessel between selected dilatations.
  • Figures 9-19 illustrate alternative embodiments of the present invention. Since these embodiments are similar to the previously described embodiment, similar parts appearing in Figures 9-19 are represented by the same, corresponding reference numeral, except for the corresponding letter in the numerals of the latter.
  • a pair of split O-ring type seals are provided to prevent inflation fluid from exiting the balloon 20a.
  • An upper portion of a proximal split O-ring 80 is attached to the curved bottom wall 40a of the catheter shaft 14a, and a lower portion is attached to the proximal neck portion 22a of the balloon 20a.
  • the entire periphery of a distal O-ring 82 can be attached to the distal seal member 64a as shown in Figure 9 or bonded directly to the distal neck portion 26a of the balloon 20.
  • the split O-rings 80 and 82 are preferably made of a relatively soft durometer urethane material or the like and can be pre-formed or molded into the balloon 20a.
  • a polyurethane adhesive or the like can be injected into a shaped mold temporarily positioned in the neck portion of the balloon 20a.
  • the contact surfaces of the O-rings 80 and 82 are shown as rounded surfaces, the O-rings can be formed in any desired shape to facilitate slidable movement of the guide lumen 44a while providing an effective seal when the balloon 20a is inflated.
  • the shape and material of the O-ring allows greater deformation as a result of pressure from the inflation fluid, which may provide a more effective seal.
  • the "single point" contact of the proximal and distal O-rings 80 and 82 with the guide lumen 44a may facilitate advancement and withdrawal of the catheter 12a over the guide lumen 44a because the decreased contact area tends to reduce frictional forces acting on the guide lumen 44a.
  • the guide lumen 44b is configured with an enclosed, deformable bladder-type sheath 84 surrounding a portion thereof.
  • the sheath 84 has a constant volume of fluid therein (not shown) and is approximately the same length as the distance between the proximal and distal seal members 62b and 64b of the balloon 20b.
  • the guide lumen 44b Prior to inflation of the balloon 20b, the guide lumen 44b is advanced or withdrawn until proximal and distal end portions 86 and 88 of the sheath 84 are substantially aligned with the proximal and distal seal members 62b and 64b ( Figure 12).
  • the sheath 84b can be provided in the form of spaced apart proximal and distal sheaths 90 and 92 surrounding the guide lumen 44c as shown in Figures 14 and 15.
  • the distance between the sheaths 90 and 92 is approximately the same as the distance between the seal members 62c and 64c.
  • the sheaths 90 and 92 are aligned with the corresponding seal members 62c and 64c prior to inflation of the balloon 20c ( Figure 14), and the inflation fluid displaces the fluid in the sheaths 90 and 92 outwardly to create a seal between the sheaths 90 and 92 and the corresponding seal members 62c and 64c.
  • the seal members can be eliminated and the sheaths can be configured to bear directly against the corresponding neck portions of the balloon when displaced by the inflation fluid.
  • a bladder-type valve member which surrounds the guide lumen 44 and expands when filled with fluid can provide an active seal.
  • Valve members of this type are disclosed in U.S. Patent No. 5,085,636, issued February 4, 1992, the disclosure of which is specifically incorporated herein by reference.
  • Such a seal could be activated by the inflation fluid which fills the balloon 20 or by a separate flow of fluid through a micro-tube connected to the bladder.
  • the proximal and distal seal members can be configured to slidably receive and provide an effective seal around a guide wire without the use of a guide lumen (see, e.g., Figure 9A).
  • One advantage of this configuration may be the reduced profile of the balloon 20 resulting from the elimination of an inner tube inside the balloon 20.
  • Such a configuration may also facilitate the flow of a radiopaque dye solution which is typically introduced into the vessel after an angioplasty procedure to determine whether an acceptable blood flow has been established through the vessel.
  • the proximal neck portion 22 preferably has an outer diameter of about 0.036 inches and an inner diameter of about 0.030 inches.
  • the distal neck portion 26 preferably has an outer diameter of about 0.025 inches and an inner diameter of about 0.020 inches.
  • the shaft 14d has a relatively large diameter body portion 100 and a smaller diameter distal end portion 102 which extends through the proximal and distal openings 24d and 28d in the balloon 20d.
  • the juncture of the body portion 100 and the distal end portion 102 is defined by a tapered shoulder 103 adjacent the balloon 20d.
  • the distal end portion 102 of shaft 14d is sealingly attached to the proximal and distal neck portions 22d and 26d of the balloon 20d.
  • the balloon 20d is inflated by conveying fluid via the inflation lumen 30d of the shaft 14d through a plurality of openings 104 formed in the distal end portion 102 of the shaft.
  • a portion of the guide lumen 44d is movably positioned within a distal portion of the inflation lumen 30d of shaft 14d.
  • the profile of catheter 12d is minimized to allow insertion into relatively small vessels.
  • the constant outer diameter of the distal end portion 102 of the shaft 14d also may provide a better joint between the balloon 20d and the shaft 14d.
  • An opening 106 is provided in the body portion 100 of the shaft 14d, preferably about 10-30 cm proximally from the balloon 20d, for receiving the guide lumen 44d.
  • the guide lumen 44d is guided by an inner core 108 which extends distally a relatively short distance, preferably about 5-15 mm, into the inflation lumen 30d from the opening 106.
  • An end portion 110 of the core 108 is flared to direct the guide lumen 44d into the core 108 when the guide lumen 44d is inserted in a proximal direction through the distal end portion 102 of the shaft 14d.
  • a seal member 110 is sealingly connected to the core 108.
  • the seal member 110 is preferably a split O-ring type seal which is described in more detail above.
  • a split O-ring type seal member 112 can also be provided in the distal neck portion 26d for sealingly engaging the guide lumen 44d.
  • the opening 106 and core 108 of the shaft 14d, along with the seal members 110 and 112, can be configured to slidably receive a guide wire or other intravascular device without the use of the guide lumen 44d.
  • the elimination of the guide lumen would allow the shaft to be configured with a smaller outer diameter, thus reducing the profile of the catheter.
  • intravascular access is initially made in a conventional manner. If the procedure is a percutaneous translumenal angioplasty (PCTA) procedure, access is made via the femoral artery.
  • PCTA percutaneous translumenal angioplasty
  • a conventional introducer and guiding catheter (not shown) can be employed in a manner that is well known in the art.
  • a guiding catheter should have a lumen of sufficient size to accommodate the catheter 12, guide lumen 44 and guide wire 54.
  • the guide wire 54 is preferably inserted into the guide lumen 44 while the entire guide lumen is outside the body such that the distal tip portion 58 of the guide wire 54 extends beyond the guide lumen 44.
  • the combination of the guide wire 54 and guide lumen 44 is then advanced to a desired location in a vessel, and the catheter 12 is advanced over the guide lumen 44.
  • the guide wire 54 can be inserted into the vessel prior to advancement of the guide lumen 44 over the guide wire, or the guide lumen 44 can be inserted into the vessel prior to advancement of the guide wire 54 through the guide lumen 44.
  • the guide wire 54 can be advanced to a desired location in a vessel in a "bare wire” technique and the catheter 12 can be passed over the guide wire 54.
  • the combination guide wire 54 and guide lumen 44 are advanced until the distal portions 48 and 58 thereof reach a distal end of the guiding catheter.
  • the guide wire 54 may be further advanced in the vessel alone, or the guide lumen 44 may be advanced along with the guide wire 54.
  • the distal portion 48 of the guide lumen 44 can provide additional support for the distal portion 58 of the guide wire 54 when desired.
  • the guide lumen 44 can then be advanced to support the guide wire 54 and assist its advancement in the vessel.
  • using the guide lumen 44 may avoid having to exchange the guide wire 54 for another guide wire having a larger diameter.
  • the guide lumen 44 is advanced until the distal end 53 reaches a distal end 60 of the guide wire 54.
  • the guide wire 54 is withdrawn from the guide lumen 44, and a desired bend can be formed in the distal portion 58 of the guide wire 54 or another guide wire can be obtained.
  • the newly configured guide wire is then advanced through the guide lumen 44 to the previously attained position.
  • the guide lumen 44 can also be used to straighten a bend in the distal portion 58 of the guide wire 54 while inside a vessel.
  • the distal portion 58 of the guide wire 54 is often bent a desired amount prior to insertion into the body of a patient to allow manipulation of the guide wire 54 through various vessels.
  • the guide wire 54 may also bend as a result of advancement of the guide wire 54 when movement of the distal tip is impeded in the vessel. If the bend is inappropriate for further advancement of the guide wire 54 to the desired location in the vessel or for advancement into a different vessel, the guide lumen 44 can be advanced over the guide wire 54 to straighten the distal portion 58 a desired amount. In addition, the guide lumen 44 can be advanced over the guide wire 54 after the guide wire is advanced past a stenosis in the vessel to pre-dilate the stenosis before insertion of the balloon 20. The guide wire 54 can also be moved within the guide lumen 44 when the balloon 20 is inflated inside a vessel.
  • a substantial portion of the guide lumen 44 and guide wire 54 is positioned outside the catheter shaft 14 to allow a single-operator exchange of the catheter 12 for a second catheter.
  • the catheter 12 is withdrawn so that the balloon 20 passes over the guide lumen 44 while an operator maintains a hold on the proximal portion 46 of the guide lumen 44 and the proximal portion 56 of the guide wire 54.
  • the balloon of a second catheter can then be advanced over the guide lumen 44 to position the second catheter in the same location previously attained by the first balloon catheter 12.
  • This single-operator exchange type configuration allows the operator to maintain a hold on the guide lumen 44 and guide wire 54 without using an extension or a relatively long guide lumen and guide wire.
  • the guide lumen 44 therefore provides for the independent or substantially contemporaneous exchange of the guide wire 54 and the catheter 12.
  • the guide wire 54 is withdrawn through the guide lumen 44 and replaced with a second guide wire.
  • the guide wire 54 can be exchanged before the catheter 12 has been inserted in the vessel, while the catheter 12 remains in the vessel, or after the catheter 12 has been withdrawn.
  • the catheter 12 can be exchanged while the guide wire 54 remains in the vessel or after the guide wire 54 has been withdrawn.
  • the position of the guide lumen 44 is maintained in the vessel by holding onto the proximal portion 46 of the guide lumen.
  • an over-the-wire type balloon dilatation catheter is indicated generally at 120.
  • the balloon catheter 120 includes an inflation tube 122 with an inflation lumen 128 extending therethrough. Attached to a distal end portion of the inflation tube 122 is an inflatable balloon 124. The interior 130 of the inflatable balloon 124 is in fluid communication with the inflation lumen 128 of the inflation tube 122, via inflation port 126. The proximal end of the inflation tube is attached to a proximal manifold 134.
  • the proximal manifold 134 includes a fluid port 136, which is in fluid communication with the inflation lumen 128 as shown.
  • the inflatable balloon 124 is expanded by applying fluid pressure to the inflation lumen 128 via fluid port 136.
  • an elongated guide member 132 may be provided.
  • the elongated guide member 132 preferably coextends interiorly within at least a portion of the inflation lumen 128, and is in a slidable relation therewith. Because the elongated guide member 132 coextends interiorly within at least a portion of the inflation lumen 128, a seal 125 is provided.
  • the seal 125 slidably receives the guide member 132 and provides a seal between the inflation lumen 128 and the exterior of the intravascular catheter 120.
  • the seal 125 comprises a seal between the inflation tube 122 and the guide member 132, as shown.
  • the seal 125 may be a friction fit seal, such as an O-ring seal.
  • the guide member 132 may be slidably positioned relative to the dilatation balloon 124.
  • an IVUS device 152 which is positioned within the guide member 132, may be slidably positioned relative to the dilatation balloon 124 (see, Figure 21). It is contemplated that a seal 138 may be provided between the manifold 134 and the guide member 132.
  • the balloon 124 is positioned adjacent an occluded site within a vessel (not shown) and inflated to dilate the occluding matter.
  • the IVUS device 152 may be advanced down the guide member 132 until the IVUS device 152 is adjacent the desired site.
  • the balloon dilatation catheter 120 may be withdrawn proximally relative to the guide member 132, as shown in Figure 22.
  • the dilatation balloon 124 is effectively moved proximally away from the IVUS device 152, and the IVUS device 152 and the guide member 132 remain adjacent the revascularized portion of the vessel.
  • the IVUS device 152 may then be used to provide an image of the occluded vessel.
  • the IVUS device 132 remains within the guide member 132 so that the guide member 132 can provide protection to the IVUS device 152. Because the guide member 132 remains across the occluded site or lesion, the balloon catheter 120 can easily be repositioned across the site by simply advancing the balloon catheter 120 over the guide member 132. This provides an efficient means for imaging a vessel between selected dilatations.
  • an illustrative method includes the steps of: providing a catheter 120 that has a movable guide member 132 therein and a balloon 124 located on the distal end thereof, wherein the catheter 120 is positioned within the body such that the balloon 124 is located adjacent a selected portion of the vessel; providing an elongated device 150 that has an imaging device 152 located near the distal end thereof, wherein the elongated device 150 is positioned within the guide member 132 as shown; moving the catheter 120 proximally of the selected portion of the vessel while leaving the movable guide member 132 substantially stationary relative to the selected portion of the vessel; positioning the imaging device 152 adjacent the selected portion of the vessel, if necessary; and imaging the selected portion of the vessel with the imaging device 152.
  • the movable guide member may have a distal portion thereof positioned distal of the balloon by actually sliding the movable guide member in a distal direction while the balloon remains substantially stationary if it is desired to image distal of the balloon. Further, it is recognized that a combination of moving the balloon catheter and associated balloon in a proximal direction and moving the movable guide member in a distal direction can also be utilized.
  • the desired results is achieved in that the movable guide member has a distal portion thereof positioned distal of the balloon of the balloon catheter for use of an imaging device.
  • a standard over-the-wire type balloon dilatation catheter is indicated generally at 162.
  • the standard balloon catheter 162 is combined with a lumen extension device 160 (see, Figure 23).
  • the lumen extension device 160 is a separate device that is used in conjunction with catheter 162.
  • the lumen extension device 160 allows a user to effectively extend the guide wire lumen of a standard catheter 162 by a selected amount.
  • the lumen extension device 160 includes an elongated guide member 170 for slidably receiving an elongated device, such as an IVUS device (not shown).
  • the guide member 170 is adapted to be slidably disposed within the guide wire lumen of the standard catheter 162.
  • a housing 172 Attached to the proximal end of the guide member 170 is a housing 172.
  • the housing 172 preferably engages the proximal end of the catheter 162, and has a control mechanism 174 for controlling the relative longitudinal position of the guide member 170 relative to the catheter 162.
  • the catheter 162 has a manifold 164 on the proximal end thereof, and the housing 172 is attached to the manifold 164, as shown in Figure 22.
  • the control mechanism 174 of the lumen extension device 160 preferably comprises a block that is slidably disposed in the housing 172.
  • the block is attached to the proximal end of the guide member 170. Attached to the block is a handle 178, and the handle 178 extends out of the housing 172 through a slot 179.
  • the handle 178 By manipulating the handle 178, the longitudinal position of the guide member 170 relative to the housing 172 may be changed, as shown at 182. Since the housing 172 is preferably mounted to a manifold 164 of catheter 162, the handle 178 may be used to change the longitudinal position of the guide member 170 relative to the catheter 162.
  • the guide member 170 may be moved proximally relative to the balloon 168, as shown at 192.
  • the guide member 170 may be moved distally relative to the balloon 168, as shown at 188.
  • the block 174 has a tapered aperture 176 for guiding an elongated device, such as a IVUS device into the guide member 170.
  • a method including the steps of: providing a catheter 162 that has a guide wire lumen extending longitudinally therethrough, and a balloon 168 located on the distal end thereof, the catheter 162 being inserted into the body such that the balloon 168 is positioned adjacent a selected portion of a vessel (not shown); providing a lumen extension device 160 comprising a elongated tube 170, wherein the lumen extension device 160 is slidably positioned within the guide wire lumen of the catheter 162; providing an elongated device (not shown) that has an imaging device located near the distal end thereof, said elongated device being positioned within the elongated tube 170 of the lumen extension device 160; moving the catheter 162 proximally of the selected portion of the vessel while leaving the lumen extension device 162 substantially stationary relative to the selected portion of the vessel; positioning the elongated device (not shown) adjacent the selected portion of the vessel, if necessary; and imaging the selected portion of the vessel with the imaging device.
  • an alternative method can include extending a distal portion of the elongated tube of the lumen extension device distal of the balloon while maintaining the balloon in a stationary position if it is desired to image distal of the balloon. Further, a combination of moving the elongated tube in a distal direction and the balloon in a proximal direction can also be utilized so that the elongated tube distal portion is positioned distal of the balloon.

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Abstract

La présente invention concerne un procédé et un appareil d'introduction de dispositifs de diagnostic et/ou thérapeutiques dans un cathéter de dilatation (12) de ballonnet et sur un site d'occlusion en déplaçant longitudinalement le ballonnet de dilatation (12) à proximité de la zone d'occlusion. Un dispositif (54) ultrasons, intra-vasculaire (IVUS), peut, par exemple, produire des images non déformées d'un site occlus entre des dilatations de ballonnet d'une procédure d'angioplastie.
PCT/US1998/004282 1997-03-06 1998-03-05 Catheter a canal de fil de guidage etirable WO1998039054A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/812,235 1997-03-06
US08/812,235 US5976107A (en) 1991-07-05 1997-03-06 Catheter having extendable guide wire lumen

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WO1998039054A1 true WO1998039054A1 (fr) 1998-09-11

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